Canonical Allele Identifier: CA743329901
Gene: AVP HGNC NCBI

Linked Data

dbSNP Id: rs1359191486
gnomAD v4: 20-3082904-G-T
MyVariant Identifiers: chr20:g.3063550G>T (hg19) chr20:g.3082904G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.3082904G>T , CM000682.2:g.3082904G>T GRCh38
NC_000020.10:g.3063550G>T , CM000682.1:g.3063550G>T GRCh37
NC_000020.9:g.3011550G>T NCBI36
NG_008663.1:g.6821C>A , LRG_715:g.6821C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000380293.3:c.322+73C>A MANE Select ENSP00000369647.3:n.322+73C>A
NM_000490.4:c.322+73C>A , LRG_715t1:c.322+73C>A NP_000481.2:n.322+73C>A
XM_011529267.1:c.322+73C>A XP_011527569.1:n.322+73C>A
XM_011529267.2:c.322+73C>A XP_011527569.1:n.322+73C>A
NM_000490.5:c.322+73C>A MANE Select NP_000481.2:n.322+73C>A
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